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Precision for Medicine is seeking a Senior Feasibility Manager to join its European Feasibility Department. This fully remote role is available across the UK, Spain, Hungary, Poland, Romania, Serbia, and Slovakia. The position combines clinical and scientific interpretation with operational intelligence and data analysis to deliver evidence-based feasibility assessments for clinical trials.
You will be responsible for leading or contributing to feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements. Key responsibilities include reviewing clinical protocols and study assumptions, conducting competitive landscape and recruitment analyses, synthesizing epidemiological and operational data, and translating evidence into clear country, site, enrollment, and operational recommendations. You will present findings and recommendations to internal stakeholders and clients, collaborate with cross-functional teams including Business Development and Clinical Operations, and coordinate targeted site and investigator outreach as needed.
The role requires strong analytical and critical-thinking skills, with the ability to synthesize multiple evidence sources and develop transparent rationales for assumptions. You will manage multiple concurrent deliverables and priorities while maintaining attention to detail and overall study strategy awareness. Experience presenting analyses to clients or senior stakeholders is valued, as is familiarity with clinical-trial intelligence platforms and real-world data sources.
You will contribute to the continued development of feasibility methods, tools, and best practices, sharing knowledge with colleagues and supporting team development. The position offers the opportunity to work across therapeutic areas and geographic regions in a matrix environment, with emphasis on scientific rigor and client-focused delivery.
Required: Bachelor's degree in life sciences or related discipline; at least two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, or clinical research; demonstrated ability to conduct feasibility analysis and site/country identification; professional English proficiency. Preferred: postgraduate degree in life sciences, public health, epidemiology, or data science; experience with global clinical trials, oncology, rare disease programs, or clinical-trial intelligence platforms; working knowledge of ICH-GCP principles.
